eTryton Left Main Registry Tryton Side Branch Stent® Tmt of Denovo CAD in LM and CFX Arteries

NCT02765646 | Unknown

• 1 other identifier: P0160
• Study Type: observational
• Target: 100
• Locations: 1 country
• Sites: 1

Brief Summary

The objective of this study is to demonstrate the clinical performance of the Tryton Side Branch Stent used in conjunction with a commercially available Drug Eluting Stent (DES) to treat de novo bifurcated lesions involving both the Left Main (LM) and Circumflex Coronary Artery(LCX).

Conditions

Left Main Coronary Artery Stenosis

Outcome Measures

Primary Outcomes (1)

• MACE: cardiac death, non-index procedure related myocardial infarction, TLR, definite stent thrombosis

  9 months

Secondary Outcomes (2)

• Procedural success: successful deployment of Tryton stent and MV DES within target lesion, Angiographic success <30% residual stenosis in LM and LAD/LCX bifurcation by visual est. and TIMI flow 3 post procedure and freedom of in-hospital MACE

  9 months

• Clinical endpoints: MACE: total death, cardiac death, non-index procedure related MI, Target lesion revascularization (TLR), Target vessel revascularization (TVR), definite stent thrombosis, Procedure related MI

  9 months

Interventions

Coronary stent procedure (CSP) DEVICE

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

Patients with CAD due to de novo stenotic lesion in the distal part of the LM at the bifurcation of the Left Anterior Descending Artery (LAD) and the Left Circumflex (LCX)

You may qualify if:

• Patient is ≥18 years old;
• Patient is eligible for percutaneous coronary intervention (PCI);
• Patient is an acceptable candidate for CABG;
• Clinical evidence of ischemic heart disease and / or a positive functional registry. Documented stable angina pectoris (Canadian cardiovascular society classification (CCS) 1, 2, 3 or 4), unstable angina pectoris (Braunwald Class IB-C, IIB-C, or IIIB-C), or documented silent ischemia;
• Single high grade de novo bifurcation lesion with ≥50% and \<100% stenosis in the distal part of left main, requiring stent placement across LCx Ostium, with TIMI flow \> 2 by visual estimation;
• The target lesion length must be able to be covered by a single main vessel stent ≥ 5.0mm and ≤ 32 mm in the main vessel and ≤ 32 mm in the side branch (visual estimate) and be covered by one Tryton stent and up to one DES in the side branch;
• The reference vessel diameter of the main branch must be ≥ 2.5mm and ≤ 4.0 mm (visual estimate) and reference vessel diameter of the side branch must be ≥ 2.25mm and ≤ 3.5 mm (visual estimate);
• If required by local regulations, the patient had been informed of the nature of the registry, agrees to its provisions and has provided written informed consent, approved by the appropriate Medical Ethics Committee (MEC) of the respective clinical site;
• The patient is willing to comply with follow-up evaluations.

You may not qualify if:

• Female of childbearing potential;
• Documented left ventricular ejection fraction (LVEF) ≤30%;
• Evidence of an acute myocardial infarction within 48 hours of the intended treatment;
• Known allergies to the following: Acetylsalicylic acid (ASA) (Aspirin®), Clopidogrel bisulfate (Plavix®.) or Ticlopidine (Ticlid®.), Heparin, contrast agent (that cannot be adequately pre-medicated);
• Acute or chronic renal dysfunction (serum creatinine \>2.0 mg/dl or \>150μmol/L);
• Target vessel has angiographic evidence of thrombus;
• Previous interventional procedure (less than 1 year) anywhere within the left main artery including the bifurcation to the LAD and/or LCX;
• Anticipated use of rotational atherectomy
• Significant (\>50%) stenosis proximal or distal to the target lesion that might require revascularization or impede run offCONFIDENTIAL Page 7 of 18 August 11, 2015 - version 5 that will not be treated during the index procedure;
• Heavily calcified lesion and/or calcified lesion which cannot be successfully predilated;
• Prior stent in the Left Main;
• Prior stent within 5mm distal of the target lesion;
• Total occluded dominant RCA;
• Trifurcation lesion with a Ramus Intermedius diameter of \>2.0 mm; a Diagonal Branch diameter of \>2.0 mm within 5 mm of LAD origin; a Obtuse Marginal \>2.0 mm diameter within 5 mm of LCx origin;
• Patient is currently participating in an investigational drug or device registry that has not completed the primary endpoint or that clinically interferes with the current registry endpoints.

Sponsors & Collaborators

• Tryton Medical, Inc.: lead

Study Sites (1)

Klinikum Cobury GmbH

Coburg, 96450, Germany

Location

Study Officials

• Stylianos A Pyxaras, MD,FESC

  Klinikum-Coburg, Germany

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: PROSPECTIVE
• Target Duration: 9 Months
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: May 3, 2016
• First Posted: May 6, 2016
• Study Start: May 1, 2016
• Primary Completion: June 1, 2019
• Study Completion: August 1, 2019
• Last Updated: April 26, 2019

Record last verified: 2019-04

Locations

DE (1)